Canonical Allele Identifier: CA2111694087

Gene: GPC6

Linked Data

• dbSNP Id: rs1890285636

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94218443T>C , CM000675.2:g.94218443T>C	GRCh38
NC_000013.10:g.94870697T>C , CM000675.1:g.94870697T>C	GRCh37
NC_000013.9:g.93668698T>C	NCBI36
NG_011880.1:g.996620T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.878-67906T>C MANE Select	ENSP00000366246.3:n.878-67906T>C
ENST00000377047.8:c.878-67906T>C	ENSP00000366246.3:n.878-67906T>C
NM_005708.3:c.878-67906T>C	NP_005699.1:n.878-67906T>C
XM_011521044.1:c.668-67906T>C	XP_011519346.1:n.668-67906T>C
NM_005708.4:c.878-67906T>C	NP_005699.1:n.878-67906T>C
XM_011521044.2:c.668-67906T>C	XP_011519346.1:n.668-67906T>C
XM_017020298.1:c.668-67906T>C	XP_016875787.1:n.668-67906T>C
XM_017020299.2:c.668-67906T>C	XP_016875788.1:n.668-67906T>C
XM_017020300.1:c.668-67906T>C	XP_016875789.1:n.668-67906T>C
XM_017020301.1:c.512-67906T>C	XP_016875790.1:n.512-67906T>C
XM_017020302.1:c.185-67906T>C	XP_016875791.1:n.185-67906T>C
NM_005708.5:c.878-67906T>C MANE Select	NP_005699.1:n.878-67906T>C